List of variants in gene combination FANCD2, FANCD2OS reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001018115.3(FANCD2):c.*3C>T	rs3172417	0.31357
NM_001018115.3(FANCD2):c.3849+13A>G	rs9811771	0.25616
NM_001018115.3(FANCD2):c.4098T>G (p.Leu1366=)	rs2272125	0.24889
NM_001018115.3(FANCD2):c.4185+33T>C	rs2272124	0.24884
NM_001018115.3(FANCD2):c.4281+115C>A	rs78896323	0.00179
NM_001018115.3(FANCD2):c.3466+10C>T	rs200208121	0.00034
NM_001018115.3(FANCD2):c.3165C>T (p.Tyr1055=)	rs375929975	0.00009
NM_001018115.3(FANCD2):c.3642T>A (p.Ser1214=)	rs538250317	0.00007
NM_001018115.3(FANCD2):c.3850-17G>T	rs369702202	0.00005
NM_001018115.3(FANCD2):c.*10A>T
NM_001018115.3(FANCD2):c.3466+6G>A
NM_001018115.3(FANCD2):c.3560+42dup	rs777197502
NM_001018115.3(FANCD2):c.3683+6G>T

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